UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020819
Receipt number R000023904
Scientific Title Evaluation of driving ability using an actual vehicle in older adults.
Date of disclosure of the study information 2016/03/01
Last modified on 2020/12/23 17:23:31

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Basic information

Public title

Evaluation of driving ability using an actual vehicle in older adults.

Acronym

Evaluation of driving ability in older adults

Scientific Title

Evaluation of driving ability using an actual vehicle in older adults.

Scientific Title:Acronym

Evaluation of driving ability in older adults

Region

Japan


Condition

Condition

Mild cognitive impairment

Classification by specialty

Psychiatry

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study was to investigate the neurobiological substrates associated with the driving ability of mild cognitive impairment using driving test and neuroimaging techniques.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The association between driving ability and neuroimaging findings.

Key secondary outcomes

Driving ability
1. Evaluation of driving skills in the same scoring method as driving test using an actual vehicle

Neuroimaging techniques include
1. Functional MRI
2. Structural MRI
3. DTI (diffusion tensor imaging)
4. NIRS (near-infrared spectroscopy)


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

Comparing the driving skill test using an actual vehicle between participants with mild cognitive impairment and healthy elderly controls.

Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

65 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1. Participants diagnosed with mild cognitive impairment at Keio University Hospital
2. Healthy controls scored more than 24 points in MMSE
3. Reliable informed consent could be obtained from the patient and or his her relatives

Key exclusion criteria

1. Participants were required to have had no lifetime history of any psychiatric disorders, or drug or alcohol misuse, as well as no neurological disorder
2. none of the participants reported unstable medical condition and history of significant head trauma.

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Masaru
Middle name
Last name Mimura

Organization

Keio University School of Medicine

Division name

Department of Neuropsychiatry

Zip code

160-8582

Address

35 Shinanomachi Shinjuku-Ku, Tokyo

TEL

03-3353-1211

Email

mimura@a7.keio.jp


Public contact

Name of contact person

1st name Bun
Middle name
Last name Yamagata

Organization

Keio University School of Medicine

Division name

Department of Neuropsychiatry

Zip code

160-8582

Address

35 Shinanomachi Shinjuku-Ku, Tokyo

TEL

03-5363-3971

Homepage URL


Email

yamagata@a6.keio.jp


Sponsor or person

Institute

Keio University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Grant-in-Aid for Scientific Research (C)

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Keio University

Address

35 Shinanomachi Shinjuku-Ku, Tokyo

Tel

03-5363-3503

Email

med-rinri-jimu@adst.keio.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2016 Year 03 Month 01 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Preinitiation

Date of protocol fixation

2016 Year 02 Month 01 Day

Date of IRB


Anticipated trial start date

2016 Year 04 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 02 Month 01 Day

Last modified on

2020 Year 12 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023904


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name